US4807402A - Diamond and cubic boron nitride - Google Patents
Diamond and cubic boron nitride Download PDFInfo
- Publication number
- US4807402A US4807402A US07/156,272 US15627288A US4807402A US 4807402 A US4807402 A US 4807402A US 15627288 A US15627288 A US 15627288A US 4807402 A US4807402 A US 4807402A
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- United States
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- mass
- carbide
- set forth
- abrasive
- support
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Classifications
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C26/00—Alloys containing diamond or cubic or wurtzitic boron nitride, fullerenes or carbon nanotubes
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J3/00—Processes of utilising sub-atmospheric or super-atmospheric pressure to effect chemical or physical change of matter; Apparatus therefor
- B01J3/06—Processes using ultra-high pressure, e.g. for the formation of diamonds; Apparatus therefor, e.g. moulds or dies
- B01J3/062—Processes using ultra-high pressure, e.g. for the formation of diamonds; Apparatus therefor, e.g. moulds or dies characterised by the composition of the materials to be processed
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B24—GRINDING; POLISHING
- B24D—TOOLS FOR GRINDING, BUFFING OR SHARPENING
- B24D18/00—Manufacture of grinding tools or other grinding devices, e.g. wheels, not otherwise provided for
- B24D18/0009—Manufacture of grinding tools or other grinding devices, e.g. wheels, not otherwise provided for using moulds or presses
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B24—GRINDING; POLISHING
- B24D—TOOLS FOR GRINDING, BUFFING OR SHARPENING
- B24D3/00—Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B30—PRESSES
- B30B—PRESSES IN GENERAL
- B30B11/00—Presses specially adapted for forming shaped articles from material in particulate or plastic state, e.g. briquetting presses, tabletting presses
- B30B11/004—Presses specially adapted for forming shaped articles from material in particulate or plastic state, e.g. briquetting presses, tabletting presses involving the use of very high pressures
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2203/00—Processes utilising sub- or super atmospheric pressure
- B01J2203/06—High pressure synthesis
- B01J2203/0605—Composition of the material to be processed
- B01J2203/062—Diamond
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2203/00—Processes utilising sub- or super atmospheric pressure
- B01J2203/06—High pressure synthesis
- B01J2203/0605—Composition of the material to be processed
- B01J2203/0645—Boronitrides
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2203/00—Processes utilising sub- or super atmospheric pressure
- B01J2203/06—High pressure synthesis
- B01J2203/065—Composition of the material produced
- B01J2203/0655—Diamond
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2203/00—Processes utilising sub- or super atmospheric pressure
- B01J2203/06—High pressure synthesis
- B01J2203/065—Composition of the material produced
- B01J2203/066—Boronitrides
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2203/00—Processes utilising sub- or super atmospheric pressure
- B01J2203/06—High pressure synthesis
- B01J2203/0675—Structural or physico-chemical features of the materials processed
- B01J2203/0685—Crystal sintering
Definitions
- the present invention generally relates to abrasive bodies and more particularly to diamond and cubic boron nitride abrasive compacts or inserts.
- Abrasive compacts are well known in the art and consist essentially of a mass of abrasive particles present in an amount of at least 70 percent by volume bonded to a hard substrate.
- the abrasive particles of compacts are invariably superabrasives, such as diamond and cubic boron nitride, and the hard substrate is usually a carbide such as tungsten carbide, titanium carbide, tantalum carbide or a mixture thereof.
- Abrasive compacts, particularly diamond and cubic boron nitride compacts may be self-bonded, i.e., the individual particles of the compact are fused and bonded together without the aid of a metal or like bonding matrix. Alternatively, compacts may be produced where there is a suitable bonding or cementing matrix present.
- Diamond and cubic boron nitride compacts can be used for the machining of metals.
- the compacts are fastened to a suitable tool support such as a shank to form a tool.
- the compacts may be fastened to a backing such as a cemented carbide backing and then the backing fastened to the support to form the tool.
- U.S. Pat. No. Re. 32,380 assigned to the same assignee as the present invention, describes a diamond compact comprising (a) a diamond crystalline mass wherein the concentration of diamond is in excess of 70 percent by volume and in which the diamond crystals are disposed in random fashion and substantially all of the diamond crystals are directly bonded to adjacent diamond crystals and (b) a support material which is a cemented carbide mass considerably larger in volume than the volume of the diamond crystalline mass, the diamond crystalline mass and the cemented carbide mass being joined at an interface consisting of cemented carbide, or its elements and diamond crystals.
- U.S. Pat. No. 3,767,371 assigned to the same assignee as the present invention, describes an analagous cubic boron nitride compact comprising (a) a unified mass of greater than 70 volume percent cubic boron nitride crystals bonded to (b) a supporting mass of metal bonded carbide selected from the group consisting of tungsten carbide, titanium carbide, tantalum carbide and mixtures thereof; the bonding material being selected from cobalt, nickel, iron and mixtures thereof and the interface between the mass of cubic boron nitride crystals and metal bonded carbide support being free of voids.
- 3,743,489 also assigned to the same assignee as the present invention, teaches that further including aluminum with the bonding medium results in superior bonding of the cubic boron nitride crystals to each other as well as between the cubic boron nitride mass and the carbide substrate.
- U.S. Pat. No. 4,224,380 assigned to the same assignee as the present invention, describes thermally stable diamond and cubic boron nitride compacts wherein the bonding material, for example cobalt or cobalt alloys, is removed so as to provide compacts having substantially 100% abrasive particles and which therefore can withstand exposure to temperatures of 1200° C. to 1300° C. without substantial thermal degradation.
- the compacts can be made only of self-bonded abrasive particles or they can be made of self-bonded particles bonded to a substrate such as cemented carbide.
- U.S. Pat. No. 4,229,186 discloses a laminated abrasive body which is in effect a thick compact comprising a plurality of diamond or cubic boron nitride compacts laminated together by means of a metal or metal alloy braze. Such laminated abrasive bodies are said to be useful as a high pressure piston in an apparatus for obtaining ultra-high pressures on the order of megabars.
- a compact comprising a support mass having abrasive masses bonded to each of the upper and lower surfaces of said support mass.
- the abrasive masses preferably are selected from diamond and cubic boron nitride and the support mass preferably is a sintered carbide.
- the abrasive masses preferably are directly bonded to the support mass, however, it is contemplated that indirect bonding, brazing for example, may also be employed in the practice of the invention.
- FIG. 1 illustrates an exemplary high pressure, high temperature apparatus useful in the preparation of the product of this invention.
- FIG. 2 illustrates in section one a form of charge assembly configuration for use within the apparatus of FIG. 1 in the practice of the instant invention.
- Apparatus 10 includes a pair of cemented tungsten carbide punches 11 and 11' and an intermediate belt or die member 12 of the same material. Die member 12 includes an aperture 13 in which there is positioned a reaction vessel 14. Between punch 11 and die 12 and between punch 11' and die 12 there are included gasketing/insulating assemblies 15 and 15', each comprising a pair of thermally insulating and electrically non-conducting pryophyllite members 16 and 17, and an intermediate metallic gasket 18.
- Reaction vessel 14 in one preferred form includes a hollow salt cylinder 19.
- Cylinder 19 may be of other material, such as talc, which is not converted during high pressure, high temperature operation to a stronger, stiffer state and is substantially free of volume discontinuities occurring under the application of high pressures and temperatures. Materials meeting the criteria set forth in U.S. Pat. No. 3,030,662, incorporated herein by reference, are useful for preparing cylinder 19.
- liner 21 Positioned concentrically within and adjacent to cylinder 19 is a graphite electrical resistance heater tube 20. Within graphite heater tube 20 there is in turn concentrically positioned the cylindrical salt liner 21. The ends of liner 21 are fitted with salt plugs 22 and 22', disposed at the top and bottom, respectively. As will be described hereinbelow, liner 21 may have a cylindrical hollow core to receive one large charge assembly containing sub-assemblies or the liner may consist of a series of mold assemblies arranged in a stack for the preparation of a plurality of composite tool inserts or compacts.
- Electrically conductive metal end discs 23 and 23' are utilized at each end of cylinder 19 to provide electrical connection to graphite heater tube 20. Adjacent each disc 23 and 23' is an end cap assembly 24 and 24', each of which comprises a phyrophyllite plug or disc 25 surrounded by an electrical conducting ring 26.
- FIG. 2 illustrates a charge assembly arrangement for producing a plurality of disc or pill-shaped composites--i.e., sintered carbide masses with a layer of abrasive, preferably diamond or cubic boron nitride, over each of the upper and lower surfaces of said sintered carbide masses.
- Charge assembly 30 consists of a cylindrical sleeve 32 of shield metal, preferably selected from the group consisting of zirconium, titanium, tantalum, tungsten and molybdenum.
- shield metal preferably selected from the group consisting of zirconium, titanium, tantalum, tungsten and molybdenum.
- Within cylindrical shield metal sleeve 32 are disposed a number of sub-assemblies protected above and below by shielding discs 33, preferably made of titanium or zirconium, and having pyrophyllite plugs 38 and 38' at the ends of said sleeve 32.
- Each sub-assembly so protected on all sides consists of a support mass 34 and an abrasive mass 36 disposed above and below said support mass 34.
- Each mass 34 can be made of a suitable support material which preferably is a carbide molding powder.
- Tungsten carbide, titanium carbide, tantalum carbide, and molybdenum carbide or a mixture thereof is most desirable, with tungsten carbide, plus cobalt powder being especially preferred.
- Each abrasive mass 36 can be any suitable abrasive material, however, diamond and cubic boron nitride are particularly preferred in the practice of the present invention.
- a transition layer (not shown) may be provided.
- This transition layer may contain both carbide powder and diamond grit in a gradated mix to minimize stress concentration as taught in U.S. Pat. Re. No. 32,380.
- an intermediate mass may be included, for example, as taught in U.S. Pat. Nos. 4,403,015 and 4,440,573, which are incorporated herein by reference.
- Other variations will, of course, be obvious to those skilled in the art.
- mass 34 preferably has a thickness of from about 0.060 inch to about 0.125 inch.
- charge assembly 30 is placed in space 31 of apparatus 10, pressure is applied thereto and the system is heated.
- the temperatures employed are in the range of from about 1200° C. to about 2000° C. for periods of time in excess of about three minutes, while at the same time, the system is subjected to very high pressure, for example, on the order of 40 kilobars or more.
- the protective sheath metal remains strongly affixed to the outer surface thereof. Exposure of the desired surfaces of the composite tool inserts is accomplished by simply grinding away the protective sheath.
- the shape of the tool inserts of the present invention need not be cylindrical, but can also be, for example, wedge-shaped, cubic, or the like.
- the present invention is not limited to tools having an abrasive mass on only the upper and lower surfaces of the support mass.
- the present invention includes, for example, cubic compacts wherein four of the six surfaces have an abrasive mass bonded thereto.
- Fine cubic boron nitride powder having a mean size of 2.5 micron and fired in ammonia at 950° C. was blended with 4 weight percent nickel aluminide (Ni 3 Al) powder having a mean size between 2 and 3 microns. Blending was performed using a one gallon attritor mill under dry conditions and using cemented tungsten carbide balls. The blended material was found to contain a very small amount of cemented carbide particles which were abraded from the mill balls. A quantity of the mixed material was loaded in a zirconium cup and leveled. Pressure was applied to obtain a uniform and dense mass of this material in the cup.
- a disc of cemented carbide was then inserted and pressed, followed by loading the same amount of cubic boron nitride powder on top of the carbide disc. Pressure was again applied in order to obtain a uniform and parallel layer of the cubic boron nitride.
- a zirconium disc of the same diameter as the cemented carbide was placed over the top layer of cubic boron nitride. The cup was then uniformly crimped. The loaded cups were then used to produce assemblies for high pressure, high temperature processing.
- the charge assembly was placed in an apparatus similar to that shown in FIG. 1, and heated at a temperature of about 1400° C. and subjected to pressure of about 70 kilobars for a period of about 18 minutes. The temperature was then lowered and the removal of pressure begun when the temperature reached about 650° C. The result was a tool insert or compact having excellent properties.
- Tool inserts manufactured in accordance with the foregoing procedure were tested for their machining performance on 4340 hardened steel relative to solid cubic boron nitride compacts and BZN compacts. In the first trial, the depth of cut was 0.02 inch and in the second trial the depth of cut was 0.05 inch. The results are set forth in TABLE 2.
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- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Manufacturing & Machinery (AREA)
- Metallurgy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Polishing Bodies And Polishing Tools (AREA)
- Powder Metallurgy (AREA)
- Ceramic Products (AREA)
- Cutting Tools, Boring Holders, And Turrets (AREA)
Abstract
Description
TABLE 1 ______________________________________ Maximum Maximum Three Point Stress Maximum Stress Stress Bend (× 1000 psi) (× 1000 psi) (× 1000 psi) Deflection BZN Compact BZN Compact Present (Inch) Carbide Up Carbide Down Invention ______________________________________ 0.01 4.2 8.4 10.6 0.02 6.8 10.1 17.7 0.03 13.5 13.5 24.5 0.04 14.8 16.9 29.6 0.05 21.1 25.3 40.6 0.06 29.6 33.8 51.5 0.07 42.2 49.0 60.0 0.075 46.5 51.5 64.9 0.08 54.9 59.1 75.2 0.09 63.4 76.0 90.8 0.10 76.0 88.7 102.2 0.11 88.7 101.4 120.8 0.12 101.4 118.3 169.0 0.13 114.0 135.2 broke ______________________________________
TABLE 2 ______________________________________ Material Removed/Flank Sample Wear (0.001 inch) ______________________________________ BZN (trial 1) 1.1 Solid CBN (trial 1) 1.2 Present Invention (trial 1) 1.4 BZN (trial 2) 1.6 Solid CBN (trial 2) 1.7 Present Invention (trial 2) 1.9 ______________________________________
Claims (23)
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US07/156,272 US4807402A (en) | 1988-02-12 | 1988-02-12 | Diamond and cubic boron nitride |
ZA889115A ZA889115B (en) | 1988-02-12 | 1988-12-05 | Diamond and cubic boron nitride abrasive compacts |
AU27533/88A AU611511B2 (en) | 1988-02-12 | 1988-12-23 | Diamond and cubic boron nitride abrasive compacts |
EP19890101115 EP0327871A3 (en) | 1988-02-12 | 1989-01-23 | Diamond and cubic boron nitride abrasive compacts |
JP1027772A JPH01274904A (en) | 1988-02-12 | 1989-02-08 | Diamond and cubic system boron nitride abrasive molded form |
KR1019890001587A KR890012757A (en) | 1988-02-12 | 1989-02-11 | Diamond and Boron Nitride Cube Polishing Compact |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US07/156,272 US4807402A (en) | 1988-02-12 | 1988-02-12 | Diamond and cubic boron nitride |
Publications (1)
Publication Number | Publication Date |
---|---|
US4807402A true US4807402A (en) | 1989-02-28 |
Family
ID=22558858
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US07/156,272 Expired - Lifetime US4807402A (en) | 1988-02-12 | 1988-02-12 | Diamond and cubic boron nitride |
Country Status (6)
Country | Link |
---|---|
US (1) | US4807402A (en) |
EP (1) | EP0327871A3 (en) |
JP (1) | JPH01274904A (en) |
KR (1) | KR890012757A (en) |
AU (1) | AU611511B2 (en) |
ZA (1) | ZA889115B (en) |
Cited By (66)
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US4985050A (en) * | 1989-08-15 | 1991-01-15 | General Electric Company | Supported thermally stable cubic boron nitride tool blanks and method for making the same |
US5015290A (en) * | 1988-01-22 | 1991-05-14 | The Dow Chemical Company | Ductile Ni3 Al alloys as bonding agents for ceramic materials in cutting tools |
AU611511B2 (en) * | 1988-02-12 | 1991-06-13 | General Electric Company | Diamond and cubic boron nitride abrasive compacts |
US5176720A (en) * | 1989-09-14 | 1993-01-05 | Martell Trevor J | Composite abrasive compacts |
US5330701A (en) * | 1992-02-28 | 1994-07-19 | Xform, Inc. | Process for making finely divided intermetallic |
US5379853A (en) * | 1993-09-20 | 1995-01-10 | Smith International, Inc. | Diamond drag bit cutting elements |
EP0680781A2 (en) * | 1994-05-06 | 1995-11-08 | General Electric Company | Supported polycrystalline compacts and method of manufacture |
US5560754A (en) * | 1995-06-13 | 1996-10-01 | General Electric Company | Reduction of stresses in the polycrystalline abrasive layer of a composite compact with in situ bonded carbide/carbide support |
WO1996036677A1 (en) * | 1995-05-15 | 1996-11-21 | Smith International, Inc. | Polycrystalline cubic boron nitride cutting tool |
US5948541A (en) * | 1996-04-04 | 1999-09-07 | Kennametal Inc. | Boron and nitrogen containing coating and method for making |
US5976716A (en) * | 1996-04-04 | 1999-11-02 | Kennametal Inc. | Substrate with a superhard coating containing boron and nitrogen and method of making the same |
US6544308B2 (en) | 2000-09-20 | 2003-04-08 | Camco International (Uk) Limited | High volume density polycrystalline diamond with working surfaces depleted of catalyzing material |
US6601662B2 (en) | 2000-09-20 | 2003-08-05 | Grant Prideco, L.P. | Polycrystalline diamond cutters with working surfaces having varied wear resistance while maintaining impact strength |
US20050050801A1 (en) * | 2003-09-05 | 2005-03-10 | Cho Hyun Sam | Doubled-sided and multi-layered PCD and PCBN abrasive articles |
US20050210755A1 (en) * | 2003-09-05 | 2005-09-29 | Cho Hyun S | Doubled-sided and multi-layered PCBN and PCD abrasive articles |
US20050230156A1 (en) * | 2003-12-05 | 2005-10-20 | Smith International, Inc. | Thermally-stable polycrystalline diamond materials and compacts |
US20050263328A1 (en) * | 2004-05-06 | 2005-12-01 | Smith International, Inc. | Thermally stable diamond bonded materials and compacts |
US20060060390A1 (en) * | 2004-09-21 | 2006-03-23 | Smith International, Inc. | Thermally stable diamond polycrystalline diamond constructions |
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US20060157285A1 (en) * | 2005-01-17 | 2006-07-20 | Us Synthetic Corporation | Polycrystalline diamond insert, drill bit including same, and method of operation |
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WO2018067505A1 (en) | 2016-10-05 | 2018-04-12 | Diamond Innovations, Inc. | Polycrystalline diamond cutter with integral polycrystalline diamond lined passage |
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US10406654B2 (en) | 2017-10-25 | 2019-09-10 | Diamond Innovations, Inc. | PcBN compact for machining of ferrous alloys |
CH715030A1 (en) * | 2018-05-29 | 2019-11-29 | Reishauer Ag | Method for producing thin abrasive bodies. |
EP3590658A1 (en) * | 2018-05-29 | 2020-01-08 | Reishauer AG | Method for producing thin grinding bodies |
WO2020005257A1 (en) | 2018-06-28 | 2020-01-02 | Diamond Innovations, Inc. | Polycrystalline diamond cutters and liquid sedimentation - hpht method of making thereof |
WO2020005261A1 (en) | 2018-06-28 | 2020-01-02 | Diamond Innovations, Inc. | Use of diamondene fragments in making polycrystalline diamond cutters and polycrystalline diamond cutters containing diamondene fragments |
WO2020131421A2 (en) | 2018-12-17 | 2020-06-25 | Diamond Innovations, Inc. | Near net shape polycrystalline diamond cutters and methods of making thereof |
Also Published As
Publication number | Publication date |
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EP0327871A3 (en) | 1991-04-03 |
AU611511B2 (en) | 1991-06-13 |
EP0327871A2 (en) | 1989-08-16 |
AU2753388A (en) | 1989-08-17 |
KR890012757A (en) | 1989-09-19 |
JPH01274904A (en) | 1989-11-02 |
ZA889115B (en) | 1989-08-30 |
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